HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → TETRAHYDROPYRAN-2-CARBONYL CHLORIDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Oxane-2-carboxylic acid | HCID 10964532 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | TETRAHYDROPYRAN-2-CARBONYL CHLORIDE | HCID 15731743 | 99.6% |
Reaction Steps
To a solution of tetrahydro-pyran-2-carboxylic acid (6.94 g, 47.96 mmol) in DCM (200 mL) are added oxalyl chloride (4.81 mL, 56.83 mmol) as a solution in DCM (50 mL) and DMF (3 drops). The reaction is stirred at room temperature for 18 h, then concentrated under reduced pressure to afford 7.1 g of tetrahydro-pyran-2-carbonyl chloride, which is used in the next step. Yield: 99%; by 58° C., 1 mm Hg; 1H NMR (250 MHz, CHLOROFORM-d) δ ppm 1.49-1.98 (5H, m), 2.02-2.19 (1H, m), 3.46-3.66 (1H, m), 3.96-4.12 (1H, m), 4.24 (1H, dd, J=9.14, 3.20 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08362039B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-d42c9243724c4120898d1e6889d4fba6 |
| Source note | uspto-grants-2013_01 |